Canonical Allele Identifier: CA1882590611
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274230G= , CM000671.2:g.133274230G= GRCh38
NC_000009.11:g.136149646G= , CM000671.1:g.136149646G= GRCh37
NC_000009.10:g.135139467G= NCBI36
NG_006669.1:g.3405C=
NG_006669.2:g.5985C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+932C=
ENST00000647353.1:n.53+932C=
ENST00000651471.1:n.63+1732C=
ENST00000679909.1:c.28+932C= ENSP00000506089.1:n.28+932C=
ENST00000453660.3:n.40+932C=
ENST00000538324.2:c.28+932C= ENSP00000483018.1:n.28+932C=
ENST00000611156.4:c.28+932C= ENSP00000483265.1:n.28+932C=
NM_020469.2:c.28+932C= NP_065202.2:n.28+932C=
NM_020469.3:c.28+932C= NP_065202.2:n.28+932C=